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is a recently described aquatic bacterium and opportunistic pathogen, closely related to and often coexisting with To study the relative abundance and population dynamics of both species in aquatic environments of cholera-endemic and cholera-free regions, we developed a multiplex qPCR assay allowing simultaneous quantification of total and (including toxigenic and O1 serogroup) cells. The presence of was restricted to samples from regions that are not endemic for cholera, where it was found at 20% of the abundance of . In this environment, non-toxigenic O1 serogroup represents almost one-fifth of the total population. In contrast, toxigenic O1 serogroup was also present in low abundance on the coast of cholera-endemic regions, but sustained in relatively high proportions throughout the year in inland waters. The majority of cells from both species were recovered from particles rather than free-living, indicating a potential preference for attached versus planktonic lifestyles. This research further elucidates the population dynamics underpinning and its closest relative in cholera-endemic and non-endemic regions through culture-independent quantification from environmental samples.
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http://dx.doi.org/10.3390/pathogens9121053 | DOI Listing |
Anal Methods
September 2025
Jilin Province Product Quality Supervision and Inspection Institute, Changchun 130103, China.
A method for determination of ten kinds of sweeteners in soybean products by multi-plug filtration cleanup (-PFC) combined with ultra-high-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) was established. The sample was extracted with acetonitrile (containing 1% formic acid), degreased by using -hexane liquid-liquid extraction and purified by solid phase extraction using an -PFC column (Oasis PRiME HLB). The analytes were separated by using a Waters ACQUITY UPLC® BEH C (2.
View Article and Find Full Text PDFMagn Reson Med
September 2025
National Institute of Mental Health, National Institutes of Health, Bethesda, Maryland, USA.
Purpose: To achieve spectrally resolved in vivo detection of glutamate, glutamine, and glutathione at 3 T.
Methods: Difference editing of N-acetylaspartate CH protons (NAA-CH) combined with a new echo-time (TE) optimization approach is introduced. Difference editing was used to detect NAA-CH independently of NAA-CH, thereby eliminating systematic errors arising from constrained fitting of the entire NAA molecule.
Research (Wash D C)
September 2025
Molecular Sensing and Imaging Center, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210023, P. R. China.
O-glycopeptides are highly expressed in various human cancers and play a key role in cancer progression and metastasis, making them promising biomarkers for early diagnostics. However, the inherent complexity and heterogeneity of glycans pose a major challenge for the simultaneous and precise analysis of multiple glycopeptides. Here, we developed a low-temperature nanopore technique capable of simultaneously discriminating 4 truncated O-glycopeptides with varied glycoforms.
View Article and Find Full Text PDFFoot Ankle Int
September 2025
Department of Radiology, School of Medicine, Keio University, Shinjuku-ku, Tokyo, Japan.
Background: Coronal wedge insoles are commonly prescribed to mitigate musculoskeletal disorders, yet their static-standing kinematic and kinetic effects on lower extremity joints remain insufficiently understood.
Methods: This cross-sectional experimental study included 15 healthy older adults (mean 64.9 ± 6.
Anal Chim Acta
November 2025
Multidisciplinary Laboratory of Food and Health (LabMAS), School of Applied Sciences (FCA), Universidade Estadual de Campinas (UNICAMP), Rua Pedro Zaccaria 1300, Limeira, 13484-350, São Paulo, Brazil. Electronic address:
Background: Monitoring industrial processes is critical for ensuring consistent product quality, as consumers expect uniformity across different production batches. In the case of herbal extracts, such as rosemary hydroalcoholic extracts, it is essential to control the yield of target compounds to maintain both the expected quality and safety. Typically, these extracts are produced in an extractor and then analyzed separately in a laboratory (offline).
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